JP2575364B2 - 微球晶性ポリアリ−レンチオエ−テル及びその製造法 - Google Patents

微球晶性ポリアリ−レンチオエ−テル及びその製造法

Info

Publication number: JP2575364B2
Authority: JP; Japan
Prior art keywords: solution; acid; polymer; pate; polyarylene thioether
Prior art date: 1986-09-05
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

JP61208899A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6363721A (ja

Inventor

幸男市川

卓之甲藤

善彌椎木

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Kureha Corp

Original Assignee

Kureha Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1986-09-05

Filing date

1986-09-05

Publication date

1997-01-22

1986-09-05 Application filed by Kureha Corp filed Critical Kureha Corp

1986-09-05 Priority to JP61208899A priority Critical patent/JP2575364B2/ja

1987-09-04 Priority to AU77995/87A priority patent/AU579526B2/en

1987-09-04 Priority to EP87307856A priority patent/EP0259189A3/de

1987-09-05 Priority to KR1019870009844A priority patent/KR920000197B1/ko

1988-03-22 Publication of JPS6363721A publication Critical patent/JPS6363721A/ja

1997-01-22 Application granted granted Critical

1997-01-22 Publication of JP2575364B2 publication Critical patent/JP2575364B2/ja

2012-01-22 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

229920000412 polyarylene Polymers 0.000 title claims description 12
238000004519 manufacturing process Methods 0.000 title claims description 11
150000003568 thioethers Chemical class 0.000 title claims description 11
229920000642 polymer Polymers 0.000 claims description 70
239000000243 solution Substances 0.000 claims description 47
239000002253 acid Substances 0.000 claims description 35
239000002585 base Substances 0.000 claims description 17
238000000034 method Methods 0.000 claims description 17
239000007864 aqueous solution Substances 0.000 claims description 15
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 14
238000006243 chemical reaction Methods 0.000 claims description 13
230000001590 oxidative effect Effects 0.000 claims description 13
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 10
150000003839 salts Chemical class 0.000 claims description 10
JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 claims description 8
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
239000000470 constituent Substances 0.000 claims description 8
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 8
229910052977 alkali metal sulfide Inorganic materials 0.000 claims description 6
239000002798 polar solvent Substances 0.000 claims description 6
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
150000001875 compounds Chemical class 0.000 claims description 5
238000004132 cross linking Methods 0.000 claims description 5
238000005987 sulfurization reaction Methods 0.000 claims description 5
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
235000019253 formic acid Nutrition 0.000 claims description 4
229910021529 ammonia Inorganic materials 0.000 claims description 3
239000002245 particle Substances 0.000 claims description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
125000000218 acetic acid group Chemical class C(C)(=O)* 0.000 claims 2
235000015250 liver sausages Nutrition 0.000 description 50
XYSQXZCMOLNHOI-UHFFFAOYSA-N s-[2-[[4-(acetylsulfamoyl)phenyl]carbamoyl]phenyl] 5-pyridin-1-ium-1-ylpentanethioate;bromide Chemical compound [Br-].C1=CC(S(=O)(=O)NC(=O)C)=CC=C1NC(=O)C1=CC=CC=C1SC(=O)CCCC[N+]1=CC=CC=C1 XYSQXZCMOLNHOI-UHFFFAOYSA-N 0.000 description 50
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 40
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 19
125000000732 arylene group Chemical group 0.000 description 9
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
238000006116 polymerization reaction Methods 0.000 description 8
239000000835 fiber Substances 0.000 description 7
239000000203 mixture Substances 0.000 description 7
239000007787 solid Substances 0.000 description 7
230000015572 biosynthetic process Effects 0.000 description 6
238000000465 moulding Methods 0.000 description 6
230000000704 physical effect Effects 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
150000007513 acids Chemical class 0.000 description 5
230000000694 effects Effects 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
229910052979 sodium sulfide Inorganic materials 0.000 description 5
GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 5
238000003786 synthesis reaction Methods 0.000 description 5
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 4
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
229920001971 elastomer Polymers 0.000 description 4
238000010128 melt processing Methods 0.000 description 4
239000012266 salt solution Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
238000004140 cleaning Methods 0.000 description 3
238000005260 corrosion Methods 0.000 description 3
230000007797 corrosion Effects 0.000 description 3
238000002425 crystallisation Methods 0.000 description 3
230000008025 crystallization Effects 0.000 description 3
238000001125 extrusion Methods 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
238000001746 injection moulding Methods 0.000 description 3
150000002576 ketones Chemical class 0.000 description 3
239000000463 material Substances 0.000 description 3
238000006386 neutralization reaction Methods 0.000 description 3
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
150000001242 acetic acid derivatives Chemical class 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
-1 alkyl ketone Chemical class 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
229920001400 block copolymer Polymers 0.000 description 2
238000000748 compression moulding Methods 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
239000003484 crystal nucleating agent Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000008188 pellet Substances 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000010935 stainless steel Substances 0.000 description 2
229910001220 stainless steel Inorganic materials 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241000694440 Colpidium aqueous Species 0.000 description 1
QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
239000005751 Copper oxide Substances 0.000 description 1
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
229910000990 Ni alloy Inorganic materials 0.000 description 1
239000002033 PVDF binder Substances 0.000 description 1
239000004696 Poly ether ether ketone Substances 0.000 description 1
229930182556 Polyacetal Natural products 0.000 description 1
239000004695 Polyether sulfone Substances 0.000 description 1
239000004697 Polyetherimide Substances 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
238000010306 acid treatment Methods 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
229920006231 aramid fiber Polymers 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
238000000071 blow moulding Methods 0.000 description 1
229920005549 butyl rubber Polymers 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
235000010216 calcium carbonate Nutrition 0.000 description 1
239000000378 calcium silicate Substances 0.000 description 1
229910052918 calcium silicate Inorganic materials 0.000 description 1
235000012241 calcium silicate Nutrition 0.000 description 1
AOWKSNWVBZGMTJ-UHFFFAOYSA-N calcium titanate Chemical compound [Ca+2].[O-][Ti]([O-])=O AOWKSNWVBZGMTJ-UHFFFAOYSA-N 0.000 description 1
OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910000431 copper oxide Inorganic materials 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
239000000806 elastomer Substances 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
235000012438 extruded product Nutrition 0.000 description 1
239000012765 fibrous filler Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
239000001095 magnesium carbonate Substances 0.000 description 1
229910000021 magnesium carbonate Inorganic materials 0.000 description 1
235000014380 magnesium carbonate Nutrition 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000012046 mixed solvent Substances 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
229920001643 poly(ether ketone) Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920006393 polyether sulfone Polymers 0.000 description 1
229920002530 polyetherether ketone Polymers 0.000 description 1
229920001601 polyetherimide Polymers 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920006124 polyolefin elastomer Polymers 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
229920001955 polyphenylene ether Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
239000004810 polytetrafluoroethylene Substances 0.000 description 1
229920002981 polyvinylidene fluoride Polymers 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000007873 sieving Methods 0.000 description 1
HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
229910010271 silicon carbide Inorganic materials 0.000 description 1
229920002050 silicone resin Polymers 0.000 description 1
229920002379 silicone rubber Polymers 0.000 description 1
239000004945 silicone rubber Substances 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
229920005992 thermoplastic resin Polymers 0.000 description 1
235000010215 titanium dioxide Nutrition 0.000 description 1
230000007704 transition Effects 0.000 description 1
239000010456 wollastonite Substances 0.000 description 1
229910052882 wollastonite Inorganic materials 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/10—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aromatic carbon atoms, e.g. polyphenylenes
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0286—Chemical after-treatment
- C08G75/0295—Modification with inorganic compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0209—Polyarylenethioethers derived from monomers containing one aromatic ring
- C08G75/0213—Polyarylenethioethers derived from monomers containing one aromatic ring containing elements other than carbon, hydrogen or sulfur
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/025—Preparatory processes
- C08G75/0254—Preparatory processes using metal sulfides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0277—Post-polymerisation treatment
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0277—Post-polymerisation treatment
- C08G75/0281—Recovery or purification
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0286—Chemical after-treatment
- C08G75/029—Modification with organic compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/02—Polythioethers; Polythioether-ethers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Inorganic Chemistry (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Compositions Of Macromolecular Compounds (AREA)

JP61208899A 1986-09-05 1986-09-05 微球晶性ポリアリ−レンチオエ−テル及びその製造法 Expired - Lifetime JP2575364B2 (ja)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
JP61208899A JP2575364B2 (ja)	1986-09-05	1986-09-05	微球晶性ポリアリ−レンチオエ−テル及びその製造法
AU77995/87A AU579526B2 (en)	1986-09-05	1987-09-04	Fine spherulitic polyarylene thioether and a process for producing the same
EP87307856A EP0259189A3 (de)	1986-09-05	1987-09-04	Feinteilige sphärulitische Polyarylenthioäther und ein Verfahren zu ihrer Herstellung
KR1019870009844A KR920000197B1 (ko)	1986-09-05	1987-09-05	미세 구과(球顆)상 폴리아릴렌 티오에테르 및 그의 제조방법

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP61208899A JP2575364B2 (ja)	1986-09-05	1986-09-05	微球晶性ポリアリ−レンチオエ−テル及びその製造法

Publications (2)

Publication Number	Publication Date
JPS6363721A JPS6363721A (ja)	1988-03-22
JP2575364B2 true JP2575364B2 (ja)	1997-01-22

Family

ID=16563971

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61208899A Expired - Lifetime JP2575364B2 (ja)	1986-09-05	1986-09-05	微球晶性ポリアリ−レンチオエ−テル及びその製造法

Country Status (4)

Country	Link
EP (1)	EP0259189A3 (de)
JP (1)	JP2575364B2 (de)
KR (1)	KR920000197B1 (de)
AU (1)	AU579526B2 (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0699559B2 (ja) *	1986-09-05	1994-12-07	呉羽化学工業株式会社	高速結晶化ポリアリーレンチオエーテルの製造法
JPH0645691B2 (ja) *	1986-09-09	1994-06-15	呉羽化学工業株式会社	ポリアリ−レンチオエ−テル組成物
JPS63146963A (ja) *	1986-12-10	1988-06-18	Kureha Chem Ind Co Ltd	封止用ポリアリ−レンチオエ−テル組成物および成形物
CA1302611C (en) *	1987-03-30	1992-06-02	Yukichika Kawakami	Polyarylene thioether composition for molding
US4877850A (en) *	1988-02-22	1989-10-31	Phillips Petroleum Company	Buffer wash of polyarylene sulfides
DE3941378A1 (de) *	1989-12-15	1991-06-20	Bayer Ag	Verfahren zur erniedrigung der kristallisationstemperatur von polyarylensulfiden
JPH1045912A (ja) *	1996-07-31	1998-02-17	Dainippon Ink & Chem Inc	ポリアリーレンスルフィドの精製方法
KR20010092962A (ko) *	2000-03-28	2001-10-27	신재균	비질과 물걸레 청소가 동시에 가능한 청소기

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2093468B (en) *	1981-02-25	1985-01-30	Toray Industries	Polyphenylenesulfide sheet-like material
US4370471A (en) *	1981-05-06	1983-01-25	Phillips Petroleum Company	Heat curing arylene sulfide polymer
DE3205992A1 (de) *	1982-02-19	1983-09-01	Bayer Ag, 5090 Leverkusen	Farbhelle polyphenylensulfide, ihre herstellung und verwendung in mischungen mit thermoplastischen polycarbonaten und/oder thermoplastischen polyestern
JPS61204267A (ja) *	1985-03-07	1986-09-10	Kureha Chem Ind Co Ltd	易結晶性アリ−レンスルフイド樹脂組成物の製造法
JPH0621168B2 (ja) *	1985-08-27	1994-03-23	呉羽化学工業株式会社	溶融結晶化温度の高いポリアリ−レンチオエ−テルの製造法
JPH0668025B2 (ja) *	1986-03-24	1994-08-31	東都化成株式会社	ポリフエニレンサルフアイドの精製方法
JPH072846B2 (ja) *	1986-04-24	1995-01-18	大日本インキ化学工業株式会社	ポリフエニレンスルフイドの製造方法
JPH0699559B2 (ja) *	1986-09-05	1994-12-07	呉羽化学工業株式会社	高速結晶化ポリアリーレンチオエーテルの製造法
JPH0645691B2 (ja) *	1986-09-09	1994-06-15	呉羽化学工業株式会社	ポリアリ−レンチオエ−テル組成物
JPH0621168A (ja) *	1992-07-02	1994-01-28	Seiko Epson Corp	プローブカード基板

1986
- 1986-09-05 JP JP61208899A patent/JP2575364B2/ja not_active Expired - Lifetime
1987
- 1987-09-04 EP EP87307856A patent/EP0259189A3/de not_active Withdrawn
- 1987-09-04 AU AU77995/87A patent/AU579526B2/en not_active Ceased
- 1987-09-05 KR KR1019870009844A patent/KR920000197B1/ko not_active Expired

Also Published As

Publication number	Publication date
JPS6363721A (ja)	1988-03-22
AU7799587A (en)	1988-03-10
EP0259189A3 (de)	1989-05-03
KR920000197B1 (ko)	1992-01-10
KR880003991A (ko)	1988-05-31
EP0259189A2 (de)	1988-03-09
AU579526B2 (en)	1988-11-24

Publication	Publication Date	Title
US4868240A (en)	1989-09-19	Polyarylene thioether of high crystallizing rate and a process for producing the same
US4820759A (en)	1989-04-11	Polyarylene thiother composition
US5290906A (en)	1994-03-01	Poly(arylene ether ketone), process for producing same and its use
EP0193951B1 (de)	1991-08-07	Verfahren zur Herstellung leicht kristallisierbarer Polyarylensulfidzusammensetzungen
JPS6345711B2 (de)	1988-09-12
JPH0621168B2 (ja)	1994-03-23	溶融結晶化温度の高いポリアリ−レンチオエ−テルの製造法
JP2575364B2 (ja)	1997-01-22	微球晶性ポリアリ−レンチオエ−テル及びその製造法
JP2505454B2 (ja)	1996-06-12	ポリアリ−レンチオエ−テル組成物
JP3190071B2 (ja)	2001-07-16	ポリアリーレンチオエーテル組成物
KR940010795B1 (ko)	1994-11-16	폴리(아릴렌 티오에테르) 수지 조성물 및 이의 압출 성형물
US4859734A (en)	1989-08-22	Composition of polyarylene thioether
JPH0517672A (ja)	1993-01-26	ケトン及びエーテル−ケトン化合物で変性したポリマー
JP3126214B2 (ja)	2001-01-22	芳香族ポリスルホンフィルム
JP3968840B2 (ja)	2007-08-29	ポリフェニレンスルフィド樹脂組成物
EP0369653A2 (de)	1990-05-23	Polyarylenthioätherketone mit verbesserter Schmelzstabilität und Verfahren zu ihrer Herstellung
KR20240105907A (ko)	2024-07-08	Pvdf 기반의 항균 조성물 및 그 제조방법
EP0323175A2 (de)	1989-07-05	Verfahren zur Behandlung von Polyphenylensulfid
JPH078545B2 (ja)	1995-02-01	高結晶化ポリアリ−レンチオエ−テル成形物
JPS6173766A (ja)	1986-04-15	ポリイミド樹脂組成物の製造方法
JPH1135822A (ja)	1999-02-09	結晶性樹脂組成物
JPH0432105A (ja)	1992-02-04	電気絶縁フィルム
JPH02214739A (ja)	1990-08-27	アロイフィルム及びその製造法
JPH0433930A (ja)	1992-02-05	ポリエーテル系共重合体樹脂成形品
JPH02199132A (ja)	1990-08-07	フィルム及びその製造法